Xiuzhi Ren
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Explore the profile of Xiuzhi Ren including associated specialties, affiliations and a list of published articles.
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34
Citations
195
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Recent Articles
1.
Yang H, Zhu W, Li B, Wang H, Xing C, Xiong Y, et al.
Orphanet J Rare Dis
. 2024 Nov;
19(1):420.
PMID: 39521996
Background: Osteogenesis imperfecta (OI) is a genetic disorder characterized by low bone mass, bone fragility and short stature. There is a significant gap in knowledge regarding the growth patterns across...
2.
Li S, Ren X, Guan Y, Zhao F, Cao Y, Geng X, et al.
Pain
. 2024 Jun;
165(9):1926-1943.
PMID: 38833577
Pathogenic variations in the NTRK1 can cause congenital insensitivity to pain with anhidrosis (CIPA), a rare autosomal recessive inherited neuropathy. The precise diagnosis of CIPA relies on the identification of...
3.
Li B, Yang H, Zhu W, Gao S, Xing C, Zhu S, et al.
Int Orthop
. 2024 Feb;
48(6):1645-1655.
PMID: 38386087
Purpose: This study explored the incidence of IRCs used in the procedures of the femur in children with osteogenesis imperfecta (OI) and investigated the independent risk factors of IRCs. Methods:...
4.
Zhu W, Xiong Y, Li B, Yang H, Xing C, Ren X, et al.
J Orthop Surg Res
. 2023 Jul;
18(1):532.
PMID: 37496046
Objective: To investigate the patient-related factors that affect the revision rate for the tibia in patients with osteogenesis imperfecta treated with the Peter-Williams nail, and to explore the relationship between...
5.
Yang H, Li B, Xing C, Gao S, Zhu W, Xiong Y, et al.
BMC Musculoskelet Disord
. 2023 Feb;
24(1):110.
PMID: 36759791
Background: Osteogenesis imperfecta (OI) is a hereditary genetic disorder characterized by bone fragility and extremity deformities. The surgical management for long-bone fractures and deformities in OI remains a challenge. We...
6.
Cao Y, Li L, Ren X, Mao B, Yang Y, Mi H, et al.
J Bone Miner Res
. 2023 Feb;
38(5):719-732.
PMID: 36734182
Osteogenesis imperfecta (OI) is a hereditary skeletal disorder that is mainly caused by variants in COL1A1/2. So far, no specific treatment has been developed to correct its underlying etiology. We...
7.
Han M, Mi H, Guan X, Ren X, Zhao X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2023 Jan;
40(2):186-190.
PMID: 36709938
Objective: To explore the genetic basis for three Chinese patients with McCune-Albright syndrome (MAS). Methods: Three children who had respectively presented at Shandong Provincial Hospital in April 2019 and Peking...
8.
Incidence and prevalence of 121 rare diseases in China: Current status and challenges: 2022 revision
Lu Y, Gao Q, Ren X, Li J, Yang D, Zhang Z, et al.
Intractable Rare Dis Res
. 2022 Oct;
11(3):96-104.
PMID: 36200031
The current study updated data on the incidence and prevalence of 121 rare diseases listed in to provide rationales and references for the development and promotion of rare-disease-related policies. The...
9.
Cao Y, You Y, Wang Q, Ren X, Li S, Li L, et al.
BMC Med Genomics
. 2022 Jul;
15(1):161.
PMID: 35842615
Background: Hypophosphatemic rickets (HR) is a rare genetic disorder associated with renal phosphate wasting and characterized by bone defects. Inactivating mutations in the phosphate regulating endopeptidase homolog X‑linked gene (PHEX)...
10.
Yang D, Ren X, Lu Y, Han J
Intractable Rare Dis Res
. 2021 Dec;
10(4):223-237.
PMID: 34877234
This review categorizes and summarizes the rare pediatric diseases that have been included in the that was jointly published by the National Health Commission and four other government departments in...